FDAFDA · Food and drugs·Recall number Z-2672-2025
Argus PB-3000, Reference Numbers: 1A.701307,3.921002, 3.921030,3.921031, 3.921006
Published October 8, 2025 · Recall initiated: August 8, 2025
Status when published: Ongoing — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
Vital sign monitoring instrument may trigger an error message during blood pressures measurements, Specifically, when the initial inflation pressure is set in the high-pressure range.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- Schiller, Ag
- Distributor
- US Nationwide distribution in the states of MT, WI, IL.
- Lot
- REF: 1A.701307: UDI- 07613365003024 REF: 3.921002, UDI: 07613365001914 REF: 3.921030, UDI: 07613365003468 REF: 3.921031: UDI: 07613365003475 REF: 3.921006, UDI: 07613365000115 Affected Serial Numbers: 7010.000160 and lower, 7012.000356 and lower, 7013.000256 and lower, 7014.000152 and lower
- Risk classification
- Class II
- Area (FDA)
- device
- Country
- Switzerland
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